Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555526718
rs1555526718
Entrez Id: 5048
Gene Symbol: PAFAH1B1
PAFAH1B1
CUI: C0431375
Disease:
Classical Lissencephaly
TA 0.700 CausalMutation CLINVAR